rs2819945

Positions:

• chr10-80193200-G-A
• chr10-80193200-G-C

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_145868.2(ANXA11):​c.-58+12143C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.487 in 151,986 control chromosomes in the GnomAD database, including 18,914 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.49 (18914 hom., cov: 32)
• Consequence: ANXA11 NM_145868.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.144

Genes affected

ANXA11 (HGNC:535): (annexin A11) This gene encodes a member of the annexin family, a group of calcium-dependent phospholipid-binding proteins. Annexins have unique N-terminal domains and conserved C-terminal domains, which contain calcium-dependent phospholipid-binding sites. The encoded protein is a 56-kD antigen recognized by sera from patients with various autoimmune diseases. Several transcript variants encoding two different isoforms have been identified. [provided by RefSeq, Dec 2015]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.92).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.631 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
ANXA11	NM_145868.2	c.-58+12143C>T		intron_variant		ENST00000422982.8	NP_665875.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
ANXA11	ENST00000422982.8	c.-58+12143C>T		intron_variant		1	NM_145868.2	ENSP00000404412	P2

Frequencies

GnomAD3 genomes AF: 0.487 AC: 73910 AN: 151868 Hom.: 18875 Cov.: 32

Gnomad AFR AF: 0.637

Gnomad AMI AF: 0.486

Gnomad AMR AF: 0.367

Gnomad ASJ AF: 0.504

Gnomad EAS AF: 0.320

Gnomad SAS AF: 0.399

Gnomad FIN AF: 0.455

Gnomad MID AF: 0.525

Gnomad NFE AF: 0.446

Gnomad OTH AF: 0.457

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.487 AC: 74000 AN: 151986 Hom.: 18914 Cov.: 32 AF XY: 0.482 AC XY: 35823 AN XY: 74268

Gnomad4 AFR AF: 0.637

Gnomad4 AMR AF: 0.367

Gnomad4 ASJ AF: 0.504

Gnomad4 EAS AF: 0.321

Gnomad4 SAS AF: 0.401

Gnomad4 FIN AF: 0.455

Gnomad4 NFE AF: 0.446

Gnomad4 OTH AF: 0.456

Alfa AF: 0.449 Hom.: 26456

Bravo AF: 0.485

Asia WGS AF: 0.406 AC: 1416 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
CADD	Benign	3.9
DANN	Benign	0.76

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Other links and lift over

dbSNP: rs2819945; hg19: chr10-81952956;